Banophen
- Product NDC
- 63629-9451
- 11-digit product format
- 636299451
- Labeler code
- 63629
- Product ID
- 63629-9451_d7617004-3047-400c-ac70-52653dd62808
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- diphenhydramine hcl
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- M012
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2009-11-02
- Marketing end
- 2028-01-31
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Banophen
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 50 mg/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-9451-1 | Banophen | 30 in 1 BOTTLE | CAPSULE | 30 | | 106 |
| 63629-9451-2 | Banophen | 60 in 1 BOTTLE | CAPSULE | 60 | | 106 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-9451 | BANOPHEN (DIPHENHYDRAMINE HCL) CAPSULE [BRYANT RANCH PREPACK] | 105 | Current NDC, Legacy NDC, 2 package rows | 20240511_d0f4b9f4-e727-4d47-b156-7bcdcb1606da.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-9451-1 | 63629945101 | 30 CAPSULE in 1 BOTTLE (63629-9451-1) | 30 capsule | 2022-09-26 | 0000-00-00 | No | No | Current |
| 63629-9451-2 | 63629945102 | 60 CAPSULE in 1 BOTTLE (63629-9451-2) | 60 capsule | 2022-09-26 | 2028-01-31 | No | No | Current |